Introduction:
Borderline resectable cholangiocarcinoma (CCA) carries a poor prognosis because many patients cannot undergo curative surgery. Following the approval of gemcitabine–cisplatin–durvalumab (GCD) in advanced biliary tract cancer, this real-world study evaluated its role as neoadjuvant therapy to improve resectability in borderline resectable CCA.
Why was this study needed?
- Borderline resectable cholangiocarcinoma has low rates of curative resection.
- Downstaging with neoadjuvant therapy may improve surgical eligibility and long-term survival.
- The efficacy of gemcitabine–cisplatin–durvalumab in the neoadjuvant setting has not been well established.
- Real-world data are needed before prospective trials become available.
- Biomarkers predicting response to neoadjuvant immunotherapy remain undefined.
Results:
- Neoadjuvant GCD enabled curative surgical resection in 46.2% of patients with anatomically or biologically borderline resectable cholangiocarcinoma, demonstrating meaningful conversion to surgery.
- All resected patients experienced tumor size reduction, with 83.3% achieving stable disease and 16.7% partial response radiologically, while pathological responses ranged from minimal to complete.
- Patients who underwent resection had significantly longer overall survival than those who remained unresectable, supporting the value of successful conversion to surgery after neoadjuvant treatment.
Clinical Impact:
This real-world experience suggests that gemcitabine–cisplatin–durvalumab is a feasible and well-tolerated neoadjuvant strategy for carefully selected patients with borderline resectable cholangiocarcinoma. The encouraging conversion-to-resection rate supports further prospective evaluation, while the heterogeneous pathological responses highlight the need for predictive biomarkers to optimize patient selection.
Bottom Line:
Neoadjuvant gemcitabine–cisplatin–durvalumab converted nearly half of borderline resectable cholangiocarcinoma patients to curative surgery and was associated with improved survival in those successfully resected. These findings support further investigation of immunotherapy-based neoadjuvant approaches in biliary tract cancer.